Linked Data
ClinVar Variation Id:
1770460
ClinVar RCV Id:
RCV002387808
dbSNP Id:
rs371428597
gnomAD v3:
4-127921529-G-A
gnomAD v4:
4-127921529-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.127921529G>A , CM000666.2:g.127921529G>A | GRCh38 |
| NC_000004.11:g.128842684G>A , CM000666.1:g.128842684G>A | GRCh37 |
| NC_000004.10:g.129062134G>A | NCBI36 |
| NG_008657.1:g.49456C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296468.8:c.1345C>T | ENSP00000296468.3:p.Pro449Ser | |
| ENST00000509826.2:c.*666C>T | ENSP00000421176.2:n.*666C>T | |
| ENST00000513559.6:c.1063C>T | ENSP00000425000.2:p.Pro355Ser | |
| ENST00000515130.6:c.*230C>T | ENSP00000493056.1:n.*230C>T | |
| ENST00000641025.1:c.*230C>T | ENSP00000493346.1:n.*230C>T | |
| ENST00000641092.1:c.*230C>T | ENSP00000493392.1:n.*230C>T | |
| ENST00000641133.1:c.*659C>T | ENSP00000493192.1:n.*659C>T | |
| ENST00000641146.1:n.1211C>T | ||
| ENST00000641147.1:c.895C>T | ENSP00000493133.1:p.Pro299Ser | |
| ENST00000641178.1:c.1210C>T | ENSP00000492989.1:p.Pro404Ser | |
| ENST00000641186.1:c.1231C>T | ENSP00000493347.1:p.Pro411Ser | |
| ENST00000641228.1:c.*230C>T | ENSP00000493194.1:n.*230C>T | |
| ENST00000641332.1:c.*406C>T | ENSP00000493397.1:n.*406C>T | |
| ENST00000641340.1:c.*474C>T | ENSP00000493191.1:n.*474C>T | |
| ENST00000641388.1:n.592C>T | ||
| ENST00000641393.1:c.895C>T | ENSP00000493197.1:p.Pro299Ser | |
| ENST00000641397.1:c.*230C>T | ENSP00000493406.1:n.*230C>T | |
| ENST00000641413.1:c.270C>T | ||
| ENST00000641434.1:c.1345C>T | ENSP00000493279.1:p.Pro449Ser | |
| ENST00000641464.1:c.*578C>T | ENSP00000493438.1:n.*578C>T | |
| ENST00000641482.1:c.*230C>T | ENSP00000493277.1:n.*230C>T | |
| ENST00000641508.1:c.*578C>T | ENSP00000493209.1:n.*578C>T | |
| ENST00000641509.1:c.1030C>T | ENSP00000493459.1:p.Pro344Ser | |
| ENST00000641590.1:c.*230C>T | ENSP00000493132.1:n.*230C>T | |
| ENST00000641658.1:c.*510C>T | ENSP00000492987.1:n.*510C>T | |
| ENST00000641686.2:c.1345C>T MANE Select | ENSP00000493218.2:p.Pro449Ser | |
| ENST00000641690.1:c.1144C>T | ENSP00000492966.1:p.Pro382Ser | |
| ENST00000641742.1:c.*510C>T | ENSP00000493315.1:n.*510C>T | |
| ENST00000641748.1:c.1345C>T | ENSP00000493330.1:p.Pro449Ser | |
| ENST00000641753.1:c.1172C>T | ||
| ENST00000641774.1:c.*597C>T | ENSP00000492960.1:n.*597C>T | |
| ENST00000641830.1:c.577C>T | ||
| ENST00000641843.1:c.*406C>T | ENSP00000493174.1:n.*406C>T | |
| ENST00000641869.1:c.546C>T | ||
| ENST00000641870.1:c.*406C>T | ENSP00000493044.1:n.*406C>T | |
| ENST00000641882.1:c.*510C>T | ENSP00000493301.1:n.*510C>T | |
| ENST00000641928.1:c.*474C>T | ENSP00000493418.1:n.*474C>T | |
| ENST00000641949.1:c.554-693C>T | ENSP00000492891.1:n.554-693C>T | |
| ENST00000642012.1:n.1209C>T | ||
| ENST00000642034.1:c.*230C>T | ENSP00000493285.1:n.*230C>T | |
| ENST00000642042.1:c.1345C>T | ENSP00000493260.1:p.Pro449Ser | |
| ENST00000642078.1:c.*406C>T | ENSP00000492885.1:n.*406C>T | |
| ENST00000296468.7:c.1345C>T | ENSP00000296468.3:p.Pro449Ser | |
| ENST00000504126.1:n.373C>T | ||
| ENST00000513559.5:c.1210C>T | ENSP00000425000.1:p.Pro404Ser | |
| ENST00000515130.5:n.1687C>T | ||
| NM_152778.2:c.1345C>T | NP_689991.1:p.Pro449Ser | |
| XM_005262893.1:c.1345C>T | XP_005262950.1:p.Pro449Ser | |
| XM_005262896.1:c.1198C>T | XP_005262953.1:p.Pro400Ser | |
| XM_005262897.1:c.1144C>T | XP_005262954.1:p.Pro382Ser | |
| XM_005262898.2:c.*230C>T | XP_005262955.1:n.*230C>T | |
| XM_011531830.1:c.1231C>T | XP_011530132.1:p.Pro411Ser | |
| XM_011531831.1:c.1030C>T | XP_011530133.1:p.Pro344Ser | |
| XM_011531832.1:c.*230C>T | XP_011530134.1:n.*230C>T | |
| XR_938717.1:n.1422C>T | ||
| NM_001363520.1:c.1144C>T | NP_001350449.1:p.Pro382Ser | |
| NM_001363521.1:c.1030C>T | NP_001350450.1:p.Pro344Ser | |
| XM_005262898.3:c.*230C>T | XP_005262955.1:n.*230C>T | |
| XM_017007989.1:c.*230C>T | XP_016863478.1:n.*230C>T | |
| XM_024453981.1:c.1210C>T | XP_024309749.1:p.Pro404Ser | |
| XM_024453982.1:c.1096C>T | XP_024309750.1:p.Pro366Ser | |
| XM_024453983.1:c.895C>T | XP_024309751.1:p.Pro299Ser | |
| XR_001741194.1:n.1318C>T | ||
| XR_001741195.1:n.1204C>T | ||
| XR_001741196.1:n.1117C>T | ||
| XR_001741197.1:n.1277C>T | ||
| XR_001741198.2:n.1173C>T | ||
| XR_001741199.1:n.1173C>T | ||
| XR_938717.2:n.1422C>T | ||
| NM_001363520.2:c.1144C>T | NP_001350449.1:p.Pro382Ser | |
| NM_001363521.2:c.1030C>T | NP_001350450.1:p.Pro344Ser | |
| NM_001371590.1:c.1210C>T | NP_001358519.1:p.Pro404Ser | |
| NM_001371591.1:c.1345C>T | NP_001358520.1:p.Pro449Ser | |
| NM_001371592.1:c.1351C>T | NP_001358521.1:p.Pro451Ser | |
| NM_001371593.1:c.1231C>T | NP_001358522.1:p.Pro411Ser | |
| NM_001371594.1:c.1198C>T | NP_001358523.1:p.Pro400Ser | |
| NM_001371595.1:c.1063C>T | NP_001358524.1:p.Pro355Ser | |
| NM_001371596.2:c.1345C>T MANE Select | NP_001358525.1:p.Pro449Ser | |
| NM_152778.3:c.1345C>T | NP_689991.1:p.Pro449Ser | |
| NM_152778.4:c.1345C>T | NP_689991.1:p.Pro449Ser |